ライフサイエンスコーパス: lobed

1 eaf shape likely derived from a more complex lobed ancestral state that persists in extant Arabidopsi

2 h from a simple polyhedral shape into highly lobed and interdigitated cells.

3 DENND1B-S is bi-lobed, and interactions with Rab35 are through conserved

4 hipod Paraphronima gracilis has a pair of bi-lobed apposition compound eyes, each with a large upward

5 actinomycetemcomitans developed asymmetric, lobed biofilm colonies that displayed complex architectu

6 n Patagonia, featuring highly inflated, five-lobed calyces, as a newly identified species of the deri

7 The cellular and molecular control of a lobed cell morphology is currently thought to involve PI

8 the transition from simple cell geometry to lobed cells.

9 The mushroom bodies are prominent lobed centers in the forebrain, or protocerebrum, of mos

10 ies that have undergone evolved loss, paired lobed centers referred to as "mushroom bodies" occur acr

11 s lead to a model for the development of the lobed chlamydial inclusion.

12 The EJC core is a four-lobed complex with a central channel and dimensions cons

13 ne in the organization of actin filaments in lobed cotyledon pavement cells and the highly elongated

14 The binding cavities are two lobed, exhibiting two opposing pockets, each lined with

15 logical data indicate that digits emerged in lobed fins of early tetrapods, which were polydactylous.

16 ng ray-finned fish, regenerates its pectoral lobed fins with a remarkable accuracy.

17 e of the ABC transporter BtuCD, reveals a bi-lobed fold resembling that of the ferrichrome binding pr

18 tion in grape leaves, which within a palmate-lobed framework exhibit diverse patterns of blade outgro

19 e prevents the nucleus, which becomes highly lobed, from physically blocking the intracellular bridge

20 raging of the tail fiber maps revealed a two-lobed globular structure at the distal end of each long

21 Lobed inclusions developed in cells infected at very low

22 The mushroom bodies of the insect brain are lobed integration centers made up of tens of thousands o

23 he prominent phenotype of the ago7 mutant is lobed leaf margins and more widely spaced lateral organs

24 We demonstrate that lobed leaf morphology is produced in a dose-dependent ma

25 nt, as breeders have selected for entire and lobed leaf morphs resulting from a single locus, okra (l

26 a role for the gene in patterning the highly lobed leaf of the poppy.

27 pression of PALM1 effectively suppresses the lobed leaf phenotype from overexpression of a class 1 KN

28 We characterized the developmental roles of lobed leaflet1 by analyzing a recessive mutant in the mo

29 bidopsis thaliana argonaute7 (AGO7), Mt-AGO7/lobed leaflet1, is required for the biogenesis of a tran

30 produces a variety of phenotypes, including lobed leaves and ectopic stipules and meristems in the s

31 The shootlike features of the lobed leaves are consistent with the normal domain of KN

32 the stage of leaf development that produces lobed leaves in response to KN1.

33 Lobed leaves may be a labile intermediate step between d

34 function in Arabidopsis results in rounded, lobed leaves with shorter and wider petioles, overexpres

35 symmetric1 (as1) or asymmetric2 (as2) showed lobed leaves, ectopic stipules in the sinuses and defect

36 ower development; plants produce distinctive lobed leaves, with occasional ectopic meristems on the v

37 in Arabidopsis transforms simple leaves into lobed leaves.

38 A six-lobed membrane spanning cellulose synthesis complex (CSC

39 hibited classical Kranz anatomy with lightly lobed mesophyll cells having low chloroplast coverage.

40 sible transformation between four- and three-lobed molecules has been induced by current injection.

41 Furthermore, a triangular or tri-lobed morphology was clearly visualized in a subset of t

42 Their subunits contain a two-lobed N-terminal domain (NTD) that comprises over 40% of

43 g parameters uniquely inherent in the double-lobed nature of the Double-Helix Point Spread Function,

44 o be either multinucleate or possessed multi-lobed nuclei that are normally located at the periphery

45 of individuals with SGD display atypical bi-lobed nuclei, lack expression of all secondary and terti

46 Paired lobed or dome-like neuropils characterize the first brai

47 scopy reconstructions show that eIF3, a five-lobed particle, interacts with the hepatitis C virus (HC

48 preading legionellae appear in an amorphous, lobed pattern that is most manifest at 25 to 30 degrees

49 In the leaf epidermis, intricately lobed pavement cells use Rho of plants (ROP) small GTPas

50 E1 assembles as a bi-lobed, presumably double hexameric structure on duplex D

51 olecules of Cas1 (Cas2/32:Cas14) into a four-lobed propeller-shaped structure, where the two Cas2 dom

52 oordinated growth between interconnected and lobed regions of neighboring petal primordia, and betwee

53 ls, CSCs exist in the plasma membrane as six-lobed rosettes that contain at least three different cel

54 The two-lobed Rrp44 protein binds to the RNase PH domain side of

55 n and morphogenesis to its characteristic bi-lobed shape between the 2- and 3-fold stages of embryoge

56 ic growth until development of the mature bi-lobed shape was completed.

57 Leaf epidermal cells have lobed shapes, which are thought to arise through a micro

58 We propose that the lobed structure is a result of division of inclusions oc

59 In the procyclic stage, a bi-lobed structure is found adjacent to the single ER exit

60 n ubiquitin ligase WWP1/AIP5 maintains a two-lobed structure like the HECT domain of the human ubiqui

61 ere, we found TbCentrin2 in an additional bi-lobed structure near to the Golgi apparatus.

62 w that, in the absence of ifenprodil, the bi-lobed structure of GluN2 ATD adopts an open conformation

63 Restriction of domain movement in the bi-lobed structure of the GluN2B ATD, by engineering of an

64 us outer capsid protein sigma3 reveals a two-lobed structure organized around a long central helix.

65 h only the first two subdomains of the three-lobed structure that is typical of canonical FERM domain

66 The development of this lobed structure was investigated in HeLa cells infected

67 r tandem beta-trefoil domains that form a bi-lobed structure with approximate pseudo 2-fold symmetry.

68 SmyD3 has a two-lobed structure with the substrate binding cleft located

69 itory aptamers analyzed have a predicted tri-lobed structure.

70 specific inner and outer radii, or multiple lobed structures.

71 ion to study the development of these unique lobed structures.

72 chemical vapor deposition (CVD) growth of 2-lobed symmetrical curvilinear graphene domains specifica

73 is TAFs is largely consistent with the three-lobed topological map for yeast TFIID, which suggests th

74 The Mre11 dimer adopts a four-lobed U-shaped structure that is critical for proper MRN